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Shift QC Analyst (Quality Control) working with a globally leading pharmaceutical manufacturing company which is present in more than 20 countries world-wide, and over 20,000 employees globally.
This QC Analyst role is working a 4 on 4 off shift pattern and is offering between 25,000 - 30,000 base salary (experience dependant), plus an additional 35% shift allowance (8,750-10,500) and a benefits package including a competitive pension, private healthcare plan, up to 15% performance related annual bonus, annual pay review, flexible working opportunity, 25.5 days annual leave plus bank holidays (with an additional day after 5, 10 and 15 years' service), 4 weeks full sick pay, income protection, business and personal travel insurance, life assurance up to 4x base salary, cycle to work scheme and more!
Taking this opportunity as QC Analyst would mean working for a leading global producer of API's (Active Pharmaceutical Ingredients). This role would include opportunities to advance your career, skillset, and education.
Responsibilities of the QC Analyst will include:
- You will be responsible for the Analysis of raw materials and product to established SOPs, alongside critical interpretation of analytical data.
- You will communicate and appropriately document analysis, and checking of analytical data.
- The QC Analyst will perform daily / weekly calibrations / monitoring of analytical apparatus alongside the preparation of customer standards/samples and related documentation.
- Responsible for updates to analytical databases and spreadsheets, whilst carrying out laboratory housekeeping, standard assessments and document generation and reviews.
- You will comply with all COSHH regulations and safe lab practices whilst carrying out basic troubleshooting and maintenance of analytical systems.
To be successful in this position as QC Analyst :
- You will hold an either a HNC/HND or a degree in a relevant Analytical, Chemical or Pharmaceutical
- Have an established technical Laboratory background including proven experience of GC (Gas Chromatography) and HPLC
- Experience in dealing with analytical reports and instrumental trouble shooting on a GMP site is also essential.
Please apply directly for this QC Analyst role.
